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将血卟啉衍生物瘤内注射到大鼠脑肿瘤后,肿瘤及正常脑组织中的荧光定位

Fluorescence localization in tumour and normal brain after intratumoral injection of haematoporphyrin derivative into rat brain tumour.

作者信息

Hebeda K M, Wolbers J G, Sterenborg H J, Kamphorst W, van Gemert M J, van Alphen H A

机构信息

Department of Neurosurgery, Free University Hospital, Amsterdam, Netherlands.

出版信息

J Photochem Photobiol B. 1995 Jan;27(1):85-92. doi: 10.1016/1011-1344(94)07056-t.

Abstract

In the intracerebral 9L rat gliosarcoma, the spatial distribution of the photosensitizer haematoporphyrin derivative (HpD) was studied after intratumoral injection. The fluorescence volume was measured in histological sections from 10 min up to 5 days after injection. Complete sensitization of the tumours could not be achieved by slow stereotactical injection of 4 mm3 HpD (mean HpD fluorescence volume, 13 +/- 11 mm3). Larger parts of the tumour could be loaded with HpD (39 +/- 23 mm3, p = 0.0001) by increasing the injection velocity and the volume to 50 mm3. Again, complete sensitization of the tumours was not achieved during a time scale of 5 days after intratumoral injection. Although the fluorescence volume did not change significantly with time, it was influenced by the injection site within the tumour. Injection of HpD within 1 mm from the tumour border resulted in significantly smaller fluorescence volumes in the tumour than injection into the tumour centre. Large injection volumes caused an increased leakage of HpD to normal brain, leading to the loss of selectivity of photosensitizer content and the occurrence of dark toxicity of normal brain while the tumours still appeared vital.

摘要

在大鼠脑内9L神经胶质瘤模型中,研究了瘤内注射光敏剂血卟啉衍生物(HpD)后的空间分布情况。在注射后10分钟至5天内,对组织切片中的荧光体积进行了测量。通过缓慢立体定向注射4立方毫米的HpD(平均HpD荧光体积为13±11立方毫米),无法实现肿瘤的完全致敏。通过将注射速度和体积增加到50立方毫米,可使更大比例的肿瘤组织摄取HpD(39±23立方毫米,p = 0.0001)。同样,在瘤内注射后的5天时间内,仍未实现肿瘤的完全致敏。虽然荧光体积随时间无显著变化,但受肿瘤内注射部位的影响。在距肿瘤边界1毫米内注射HpD,肿瘤内的荧光体积显著小于注射到肿瘤中心的情况。大剂量注射会导致HpD向正常脑组织的渗漏增加,导致光敏剂含量的选择性丧失以及正常脑组织出现暗毒性,而此时肿瘤仍显示存活。

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